Authors: Dan Shen, Jingyi Chu, Xiaolin Zhou, Zejun Lan, Rulan Zhang, Shuyu Wang, Haoxuan Tang, Yunrui Wang, Chenlei Hu, Zhiyuan Li, and Yan Song.
Journal: PNAS
DOI: 10.1073/pnas.2527895123
Link: https://doi.org/10.1073/pnas.2527895123
Published: Oct, 4, 2025
Document Type: Research Article
Abstract:
Differentiation programs actively lock neurons into a terminally differentiated state. How differentiation programs operate in distinct neuronal lineages remains obscure. Here, we found that previously well-characterized Drosophila neuronal differentiation factors are specifically expressed in the central brain late-born neurons but not early-born neurons, indicating the existence of a distinct, early differentiation program. We next identified T cell factor (TCF) and Odd-paired (Opa)/Zic as part of the early differentiation program that is specifically expressed in the early-born neurons to prevent neuronal dedifferentiation, partly through restricting Chinmo expression. At the molecular level, TCF promotes neuronal differentiation through a Wnt-independent noncanonical mode, via forming a transcriptional complex with Opa. Together, our study unveils that distinct differentiation programs operate in fly central brain early-born versus late-born neurons. Such customized differentiation mechanism whereby temporal differentiation programs safeguard their corresponding temporal identity specification programs is likely to also operate in mammalian brain development.